scholarly article | Q13442814 |
P356 | DOI | 10.1016/S1074-7613(00)00025-X |
P698 | PubMed publication ID | 10981968 |
P2093 | author name string | Kappos L | |
Sonnino S | |||
Kronenberg M | |||
Mori L | |||
Chigorno V | |||
Benedict CA | |||
De Libero G | |||
Prigozy TI | |||
Donda A | |||
Shamshiev A | |||
P2860 | cites work | Structural requirements for glycolipid antigen recognition by CD1b-restricted T cells | Q42547312 |
Molecular interaction of CD1b with lipoglycan antigens | Q43559521 | ||
The mannose receptor delivers lipoglycan antigens to endosomes for presentation to T cells by CD1b molecules | Q46385893 | ||
Aggregative properties of gangliosides in solution. | Q52377219 | ||
Aggregation properties of semisynthetic GM1 ganglioside (II3Neu5AcGgOse4Cer) containing an acetyl group as acyl moiety | Q70280078 | ||
Carbohydrate Components of Extraneuronal Gangliosides from Bovine and Human Spleen, and Bovine Kidney | Q71652741 | ||
Two classes of CD1 genes | Q24293259 | ||
Crystal structure of an MHC class I presented glycopeptide that generates carbohydrate-specific CTL | Q27639768 | ||
Crystal structures of two H-2Db/glycopeptide complexes suggest a molecular basis for CTL cross-reactivity | Q27639770 | ||
Crystal structure of the human class II MHC protein HLA-DR1 complexed with an influenza virus peptide | Q27731272 | ||
Crystal structure of mouse CD1: An MHC-like fold with a large hydrophobic binding groove | Q27740401 | ||
CD1d-restricted and TCR-mediated activation of valpha14 NKT cells by glycosylceramides | Q28254991 | ||
CD1c-mediated T-cell recognition of isoprenoid glycolipids in Mycobacterium tuberculosis infection | Q28378014 | ||
CD1-restricted T cell recognition of microbial lipoglycan antigens | Q28610594 | ||
Advanced mammalian gene transfer: high titre retroviral vectors with multiple drug selection markers and a complementary helper-free packaging cell line | Q29547239 | ||
The CD1 system: antigen-presenting molecules for T cell recognition of lipids and glycolipids | Q33652486 | ||
CD1-mediated immune responses to glycolipids | Q33664794 | ||
Molecular mimicry and autoimmunity. | Q33806107 | ||
Separate pathways for antigen presentation by CD1 molecules | Q33885926 | ||
Molecular recognition of lipid antigens by T cell receptors | Q35834577 | ||
CD1d-mediated recognition of an alpha-galactosylceramide by natural killer T cells is highly conserved through mammalian evolution | Q36404242 | ||
Semisynthetic preparation of N-glycolylneuraminic acid containing GM1 ganglioside: chemical characterization, physico-chemical properties and some biochemical features | Q36451748 | ||
Geometrical and conformational properties of ganglioside GalNAc-GD1a, IV4GalNAcIV3Neu5AcII3Neu5AcGgOse4Cer. | Q36723328 | ||
Presentation of peptide antigens by mouse CD1 requires endosomal localization and protein antigen processing | Q36733819 | ||
HLA-A2-peptide complexes: refolding and crystallization of molecules expressed in Escherichia coli and complexed with single antigenic peptides | Q36954248 | ||
A transient three-plasmid expression system for the production of high titer retroviral vectors | Q40393091 | ||
Self glycolipids as T-cell autoantigens | Q40950196 | ||
The tyrosine-containing cytoplasmic tail of CD1b is essential for its efficient presentation of bacterial lipid antigens | Q41053140 | ||
Preparation of radiolabeled gangliosides | Q41172552 | ||
Cytoplasmic tail-dependent localization of CD1b antigen-presenting molecules to MIICs | Q41183877 | ||
Recognition of a lipid antigen by CD1-restricted alpha beta+ T cells. | Q41411454 | ||
CD1b restricts the response of human CD4-8- T lymphocytes to a microbial antigen | Q41939036 | ||
P433 | issue | 2 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | oligosaccharide | Q320607 |
beta-D-Gal-(1->3)-beta-D-GalNAc-(1->4)-[alpha-Neu5Ac-(2->3)]-beta-D-Gal-(1->4)-beta-D-Glc-(1<->1')-Sph | Q27131420 | ||
beta-D-Gal-(1->3)-beta-D-GalNAc-(1->4)-[alpha-Neu5Ac-(2->3)]-beta-D-Gal-(1->4)-beta-D-Glc-(1<->1')-Cer(d18:1/24:0) | Q27157980 | ||
P304 | page(s) | 255-264 | |
P577 | publication date | 2000-08-01 | |
P1433 | published in | Immunity | Q6005457 |
P1476 | title | The alphabeta T cell response to self-glycolipids shows a novel mechanism of CD1b loading and a requirement for complex oligosaccharides | |
P478 | volume | 13 |
Q60920987 | A T-cell receptor escape channel allows broad T-cell response to CD1b and membrane phospholipids |
Q34955810 | A new aspect in glycolipid biology: glycosphingolipids as antigens recognized by T lymphocytes |
Q33826848 | A novel self-lipid antigen targets human T cells against CD1c(+) leukemias |
Q38568857 | Activation of human T cells by CD1 and self-lipids. |
Q33733888 | Activation state and intracellular trafficking contribute to the repertoire of endogenous glycosphingolipids presented by CD1d [corrected] |
Q63361575 | Acylation State of the Phosphatidylinositol Mannosides fromMycobacterium bovisBacillus Calmette Guérin and Ability to Induce Granuloma and Recruit Natural Killer T Cells |
Q34415144 | Anatomy of CD1-lipid antigen complexes |
Q37499317 | Antigen Presentation by CD1 Lipids, T Cells, and NKT Cells in Microbial Immunity |
Q35159082 | Antigen presentation in vaccine development |
Q34007719 | Antigenic properties and processing requirements of 65-kilodalton mannoprotein, a major antigen target of anti-Candida human T-cell response, as disclosed by specific human T-cell clones |
Q85211735 | Association of CD1A +622 T/C, +737 G/C and CD1E +6129 A/G Genes Polymorphisms with Multiple Sclerosis |
Q35346349 | Autoreactive CD1b-restricted T cells: a new innate-like T-cell population that contributes to immunity against infection |
Q34129382 | CD1 and lipid antigens: intracellular pathways for antigen presentation |
Q37014085 | CD1 antigen presentation: how it works |
Q34815690 | CD1 tetramers: a powerful tool for the analysis of glycolipid-reactive T cells |
Q77383353 | CD1 trafficking: invariant chain gives a new twist to the tale |
Q39077675 | CD1-Restricted T Cells at the Crossroad of Innate and Adaptive Immunity |
Q35031983 | CD1-restricted antigen presentation: an oily matter |
Q33695019 | CD1: A Singed Cat of the Three Antigen Presentation Systems. |
Q35090593 | CD1a-autoreactive T cells are a normal component of the human αβ T cell repertoire |
Q60219579 | CD1a-binding glycosphingolipids stimulating human autoreactive T-cells: synthesis of a family of sulfatides differing in the acyl chain moiety |
Q92259111 | CD1b presents self and Borrelia burgdorferi diacylglycerols to human T cells |
Q40230027 | CD1b-autoreactive T cells contribute to hyperlipidemia-induced skin inflammation in mice |
Q37308220 | CD1b-autoreactive T cells recognize phospholipid antigens and contribute to antitumor immunity against a CD1b+ T cell lymphoma |
Q41903337 | CD1c presentation of synthetic glycolipid antigens with foreign alkyl branching motifs |
Q37535060 | CD1d-restricted T cell activation by nonlipidic small molecules |
Q40703013 | Calnexin, calreticulin, and ERp57 cooperate in disulfide bond formation in human CD1d heavy chain |
Q48235811 | Contact sensitizers trigger human CD1-autoreactive T-cell responses |
Q36376637 | Cross-presentation of disialoganglioside GD3 to natural killer T cells |
Q34550454 | Cross-talk between cd1d-restricted nkt cells and γδ cells in t regulatory cell response |
Q47218271 | Cutting glycolipids down to size |
Q33948634 | Dendritic cells and anergic type I NKT cells play a crucial role in sulfatide-mediated immune regulation in experimental autoimmune encephalomyelitis |
Q36403863 | Diacylated sulfoglycolipids are novel mycobacterial antigens stimulating CD1-restricted T cells during infection with Mycobacterium tuberculosis |
Q35195374 | Diverse endogenous antigens for mouse NKT cells: self-antigens that are not glycosphingolipids |
Q34053547 | Editing of CD1d-bound lipid antigens by endosomal lipid transfer proteins. |
Q58655852 | Endogenous and Exogenous CD1-Binding Glycolipids |
Q34972844 | Endogenous phosphatidylcholine and a long spacer ligand stabilize the lipid-binding groove of CD1b |
Q34983782 | Exogenous control of the expression of Group I CD1 molecules competent for presentation of microbial nonpeptide antigens to human T lymphocytes |
Q38619546 | Group 1 CD1-restricted T cells and the pathophysiological implications of self-lipid antigen recognition |
Q37859643 | Guillain-barré syndrome: modern theories of etiology. |
Q33796925 | High-frequency and adaptive-like dynamics of human CD1 self-reactive T cells |
Q36584187 | How T lymphocytes recognize lipid antigens |
Q36403172 | Human CD1-restricted T cell recognition of lipids from pollens |
Q37287214 | Immunologic glycosphingolipidomics and NKT cell development in mouse thymus. |
Q34031887 | Inhibition of glycolipid shedding rescues recognition of a CD1+ T cell lymphoma by natural killer T (NKT) cells. |
Q35038295 | Intracellular pathways of CD1 antigen presentation |
Q34085898 | Intracellular trafficking pathway of newly synthesized CD1b molecules |
Q39634192 | Invariant natural killer T cells: linking inflammation and neovascularization in human atherosclerosis |
Q37251063 | Lewis rats immunized with GM1 ganglioside do not develop peripheral neuropathy |
Q34722422 | Ligand-independent assembly of recombinant human CD1 by using oxidative refolding chromatography |
Q64946734 | Linking CD1-Restricted T Cells With Autoimmunity and Dyslipidemia: Lipid Levels Matter. |
Q92863079 | Lipid Antigen Presentation by CD1b and CD1d in Lysosomal Storage Disease Patients |
Q43950987 | Lipid length controls antigen entry into endosomal and nonendosomal pathways for CD1b presentation |
Q78010078 | Lipid presentation by CD1: the short and the long lipid story |
Q37219070 | Lysosomal recycling terminates CD1d-mediated presentation of short and polyunsaturated variants of the NKT cell lipid antigen alphaGalCer |
Q28265793 | Mini review: immune response to myelin-derived sulfatide and CNS-demyelination |
Q37582663 | Molecular and immunogenic features of myelin lipids: incitants or modulators of multiple sclerosis? |
Q47728419 | Molecular recognition of microbial lipid-based antigens by T cells. |
Q43814667 | Multiple defects in antigen presentation and T cell development by mice expressing cytoplasmic tail-truncated CD1d |
Q34288977 | NKT Cell Subsets Can Exert Opposing Effects in Autoimmunity, Tumor Surveillance and Inflammation |
Q33947957 | Natural killer T cells reactive to a single glycolipid exhibit a highly diverse T cell receptor beta repertoire and small clone size |
Q37226687 | Photoaffinity antigens for human gammadelta T cells |
Q48762668 | Potential environmental and host participants in the early white matter lesion of adreno-leukodystrophy: morphologic evidence for CD8 cytotoxic T cells, cytolysis of oligodendrocytes, and CD1-mediated lipid antigen presentation |
Q34129309 | Presentation of self and microbial lipids by CD1 molecules |
Q36370124 | Presentation of the same glycolipid by different CD1 molecules |
Q36399392 | Prevention of autoimmunity by targeting a distinct, noninvariant CD1d-reactive T cell population reactive to sulfatide |
Q37469136 | Promiscuity of MHC class Ib-restricted T cell responses |
Q36146922 | Recognition of lipid antigens by T cells |
Q34180396 | Right on target: novel approaches for the direct visualization of CD1-specific T cell responses |
Q26801636 | Role of Group 1 CD1-Restricted T Cells in Infectious Disease |
Q40600420 | Saposins facilitate CD1d-restricted presentation of an exogenous lipid antigen to T cells |
Q35470808 | Structural reorganization of the antigen-binding groove of human CD1b for presentation of mycobacterial sulfoglycolipids |
Q37994621 | T cells specific for lipid antigens |
Q37522519 | Targeting Innate-Like T Cells in Tuberculosis. |
Q55399719 | The Conventional Nature of Non-MHC-Restricted T Cells. |
Q35798152 | The Third Way: Progress on pathways of antigen processing and presentation by CD1. |
Q28593372 | The adaptor protein AP-3 is required for CD1d-mediated antigen presentation of glycosphingolipids and development of Valpha14i NKT cells |
Q34179888 | The effect of intracellular trafficking of CD1d on the formation of TCR repertoire of NKT cells |
Q37761491 | The immunological functions of saposins |
Q42554741 | The majority of CD1d-sulfatide-specific T cells in human blood use a semiinvariant Vδ1 TCR |
Q36369224 | The mouse CD1d-restricted repertoire is dominated by a few autoreactive T cell receptor families |
Q34955824 | The origin of anti-GM1 antibodies in neuropathies: the "binding site drift" hypothesis |
Q36027486 | The structural and functional role of myelin fast-migrating cerebrosides: pathological importance in multiple sclerosis. |
Q36472036 | The surprising diversity of lipid antigens for CD1-restricted T cells |
Q35879532 | Type II NKT cell-mediated anergy induction in type I NKT cells prevents inflammatory liver disease |
Q37366376 | pH-dependent interdomain tethers of CD1b regulate its antigen capture |
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